Abstract
AbstractSequence register shifts remain one of the most elusive errors in experimental macromolecular models. They may affect model interpretation and propagate to newly built models from older structures. In a recent publication I have shown that register shifts in cryo-EM models of proteins can be detected using a systematic re-assignment of short model fragments to the target sequence. Here, I show that the same approach can be used to detect register shifts in crystal structure models using standard, model-bias corrected electron-density maps. I describe in detail five register shift errors detected using the method in models deposited in the PDB.SynopsisI show thatcheckMySequence, an automated method for validating sequence assignment in cryo-EM structures of proteins, can be used for validating crystal structure models.
Publisher
Cold Spring Harbor Laboratory